Showing results (111-120 of 127) with videos related to

Sort By:
Pageof 13
Annals of Hematology|March 21, 2024
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case reportJian-Hui Zhang, Hui Chen, Dan-Dan Ruan, et al.
Thrombosis Journal|January 9, 2023
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiencyHan-Lu Wang, Dan-Dan Ruan, Min Wu, et al.
Pediatric Rheumatology Online Journal|October 23, 2023
Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritisShi-Jie Li, Dan-Dan Ruan, Wei-Zhen Wu, et al.
BMC Cardiovascular Disorders|September 30, 2025
A novel NOTCH1 nonsense variant in a bicuspid aortic valve family with intrafamilial clinical heterogeneityQian Chen, Zi-Yan Xu, Wu Chi, et al.
International Immunopharmacology|November 25, 2025
Fasudil targets the RhoA/ROCK-NLRP3 axis to attenuate aristolochic acid-induced renal pyroptosis: translational validation by in vivo molecular imagingMei-Zhu Gao, Yan-Feng Zhou, Zi-Yan Xu, et al.
Frontiers in Neuroscience|August 15, 2024
In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonismDan-Dan Ruan, Jing Zou, Li-Sheng Liao, et al.
Digestive Diseases and Sciences|April 2, 2024
Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous CarrierJian-Hui Zhang, Ai-Ping Lin, Li Zhang, et al.
Experimental and Therapeutic Medicine|July 9, 2025
Genetic and clinical insights into acute kidney injury in maturity-onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitorsJing Zou, Xiang Chen, Hong-Ping Yu, et al.
Acta Histochemica Et Cytochemica|July 11, 2015
Low EphA7 Expression Correlated with Lymph Node Metastasis and Poor Prognosis of Patients with Esophageal Squamous Cell CarcinomaYu-Qin Bai, Jun-Yi Zhang, Chun-Ying Bai, et al.
Medscience|February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutationsJian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.
Pageof 13